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J Hypertens ; 9(11): 1057-62, 1991 Nov.
Article in English | MEDLINE | ID: mdl-1661764

ABSTRACT

Studies in animal models have indicated that ramipril is a potent inhibitor of angiotensin converting enzyme (ACE) in serum and tissue. In our study, the normal range of ACE activity and the inhibitory effect of short-term oral administration of ramipril on ACE activity in human serum and tissue samples of renal cortex, heart and blood vessels were determined. ACE activity in the renal cortex (125.2 +/- 11.5 nmol/mg per min) was greater than 600 times that of the heart (0.20 +/- 0.01 nmol/mg per min), greater than 500 times that of the veins (0.23 +/- 0.09 nmol/mg per min) and greater than 150 times that of the arteries (0.80 +/- 0.23 nmol/mg per min). ACE activity in the renal cortex and arteries 2 h after last dosing was almost completely inhibited by ramipril whereas ACE activity in the veins and heart was inhibited to a lesser extent. Our results demonstrate in man, for the first time, an inhibition of tissue ACE following short-term oral treatment with an ACE inhibitor.


Subject(s)
Angiotensin-Converting Enzyme Inhibitors/pharmacology , Bridged Bicyclo Compounds/pharmacology , Peptidyl-Dipeptidase A/metabolism , Administration, Oral , Angiotensin II/blood , Female , Humans , Kidney Cortex/enzymology , Male , Middle Aged , Myocardium/enzymology , Ramipril , Reference Values , Renin/blood , Surgical Procedures, Operative , Time Factors
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